A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv441e199



Internal ID22758214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:24166440..24569194hg38UCSC Ensembl
chr15:24411587..24814341hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg38402755
hg19402755
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2672154, esv2670380
SamplesHG01173, NA19332
Known GenesPWRN1, PWRN2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv441e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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